Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Rabya Sayed"'
Autor:
Graham W. Taylor, Janet A. Gilbertson, Rabya Sayed, Angel Blanco, Nigel B. Rendell, Dorota Rowczenio, Tamer Rezk, P. Patrizia Mangione, Diana Canetti, Paul Bass, Philip N. Hawkins, Julian D. Gillmore
Publikováno v:
Kidney International Reports, Vol 4, Iss 7, Pp 977-986 (2019)
Introduction: Hereditary fibrinogen Aα-chain (AFib) amyloidosis is a relatively uncommon renal disease associated with a small number of pathogenic fibrinogen Aα (FibA) variants; wild-type FibA normally does not result in amyloid deposition. Proteo
Externí odkaz:
https://doaj.org/article/034578518fe347d4a2ac583d09552583
Autor:
Tamer Rezk, Rabya Sayed, Nigel B. Rendell, Janet A. Gilbertson, Philip N. Hawkins, Diana Canetti, Angel Blanco, Julian D. Gillmore, Palma Mangione, Paul Bass, Graham W. Taylor, Dorota Rowczenio
Publikováno v:
Kidney International Reports, Vol 4, Iss 7, Pp 977-986 (2019)
Kidney International Reports
Kidney International Reports
Introduction: Hereditary fibrinogen Aα-chain (AFib) amyloidosis is a relatively uncommon renal disease associated with a small number of pathogenic fibrinogen Aα (FibA) variants; wild-type FibA normally does not result in amyloid deposition. Proteo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36377956339192dfffb7a67f465968d8
http://www.sciencedirect.com/science/article/pii/S2468024919301548
http://www.sciencedirect.com/science/article/pii/S2468024919301548
Autor:
Ketna Patel, Shameem Mahmood, Marianna Fontana, Janet A. Gilbertson, Carol J. Whelan, Sajitha Sachchithanantham, Thomas Wagner, Philip N. Hawkins, Dorota Rowczenio, Julian D. Gillmore, Frank Bridoux, Helen J. Lachmann, Ashutosh D. Wechalekar, Rabya Sayed, Christopher P. Venner
Publikováno v:
The Lancet Haematology. 2:e241-e250
Summary Background Localised immunoglobulin light-chain amyloidosis, involving one type of tissue, is rare. Little systematic data exists regarding clinical presentations, course or outcomes, or risk of progression to systemic amyloidosis. We aimed t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f861d76fdcf0dcc3bddc538987bb1ad
https://doi.org/10.1016/s2352-3026(15)00068-x
https://doi.org/10.1016/s2352-3026(15)00068-x
Autor:
Sajitha Sachchithanantham, Julian D. Gillmore, Shameem Mahmood, Helen J. Lachmann, Philip N. Hawkins, Ketna Patel, Paul Bass, Carol J. Whelan, Rabya Sayed, Marianna Fontana, Janet A. Gilbertson, Ashutosh D. Wechalekar
Publikováno v:
Blood. 126(26)
Light chain deposition disease (LCDD) is characterized by the deposition of monotypic immunoglobulin light chains in the kidney, resulting in renal dysfunction. Fifty-three patients with biopsy-proven LCDD were prospectively followed at the UK Nation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af2184ced0d4083668b31ff543004976
https://pubmed.ncbi.nlm.nih.gov/26705338
https://pubmed.ncbi.nlm.nih.gov/26705338
Publikováno v:
Clinical Kidney Journal
IgG4-related tubulointerstitial nephritis is an uncommon cause of renal impairment. It has been associated with dysfunction in a number of other organs giving rise to the term IgG4-related systemic disease; organ involvement can occur metachronously,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ca545c4844b25cf1a17cfc2375fbefd
https://doi.org/10.1093/ckj/sfs187
https://doi.org/10.1093/ckj/sfs187
Autor:
Ketna S Patel, Marianna Fontana, Sajitha Sachchithanantham, Rabya Sayed, Ashutosh D Wechalekar, Helen J Lachmann, Philip N Hawkins, Carol J Whelan, Julian D Gillmore
Publikováno v:
Circulation. 130
Introduction: Cardiac transthyretin (ATTR) amyloidosis is an increasingly diagnosed cause of heart failure. Wild-type ATTR amyloidosis (ATTRwt) is a disease of older Caucasian men. Hereditary (mutant) cardiac ATTR amyloidosis (ATTRm) is most commonly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f908920b73f9d71266749b475c49d8cf
https://doi.org/10.1161/circ.130.suppl_2.16030
https://doi.org/10.1161/circ.130.suppl_2.16030
Autor:
Julian D. Gillmore, Sajitha Sachchithanantham, Ashutosh D. Wechalekar, Ketna Patel, Carol J. Whelan, Fakhar Khan, Marianna Fontana, Rabya Sayed, Helen J. Lachmann, Dominic P.S. Rogers, Shameem Mahmood, Philip N. Hawkins
Publikováno v:
European heart journal. 36(18)
Aims AL amyloidosis may respond to chemotherapy but two-thirds of patients with severe cardiac involvement die within a year of diagnosis, purportedly from tachyarrhythmias or electromechanical dissociation. We sought to characterize the nature of ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12d3bbf29d18b3cc8ee1cce58967953a
https://pubmed.ncbi.nlm.nih.gov/25549725
https://pubmed.ncbi.nlm.nih.gov/25549725
Autor:
David F. Hutt, Rabya Sayed, Janet A. Gilbertson, Helen J. Lachmann, Philip N. Hawkins, Julian D. Gillmore, Paul Bass
Publikováno v:
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association. 29(11)
BACKGROUND Minimal change disease (MCD) accounts for 10-15% of all adult nephrotic syndrome cases and requires normal renal histology by light microscopy and negative immunohistology. Foot process effacement on electron microscopy (EM) is typical. Re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad6a358726e3ac1c555c803245ad1680
https://pubmed.ncbi.nlm.nih.gov/25016607
https://pubmed.ncbi.nlm.nih.gov/25016607
Publikováno v:
Kidney international. 87(3)
Amyloidosis results from protein misfolding, and ongoing amyloid deposition can ultimately lead to organ failure and death. Historically, this is a group of diseases with limited treatment options and frequently poor prognosis. However, there are now
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::960e3bfe7a30f77a3a6dc11100ff4af4
https://pubmed.ncbi.nlm.nih.gov/25469850
https://pubmed.ncbi.nlm.nih.gov/25469850
Autor:
Ashutosh D. Wechalekar, Cristina Quarta, Carol J. Whelan, Ketna Patel, K. Gomez, Mark R.E. Coyne, Julian D. Gillmore, Sajitha Sachchithanantham, Rabya Sayed, Taryn Youngstein, Helen J. Lachmann, Thirusha Lane, Darren Foard, Shameem Mahmood, Philip N. Hawkins, A. Riddle, Marianna Fontanna
Publikováno v:
Clinical Lymphoma Myeloma and Leukemia. 15:e201
PO-206 Bleeding diathesis and prothrombotic tendencies in patients with newly diagnosed systemic light chain Amyloidosis: important clinical implications S. Mahmood, A. Riddle, S. Sachchithanantham, T. Lane, D. Foard, T. Youngstein, R. Sayed, K. Pate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f077c6355fe1a2a453278ac5fc82e64f
https://doi.org/10.1016/j.clml.2015.07.439
https://doi.org/10.1016/j.clml.2015.07.439